Anke Abt Email & Phone Number
@3r-lifescience.de
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Who is Anke Abt? Overview
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Anke Abt is listed as Qualitätsmanagement, Regulations und Prozess-Digitialisierung at 3R LifeScience GmbH, a with 7 employees, based in Berlin, Germany. AeroLeads shows a work email signal at 3r-lifescience.de and a matched LinkedIn profile for Anke Abt.
Anke Abt previously worked as Quality Management and Regulations at 3R Lifescience Gmbh and Quality Manager at Dreve Prodimed Gmbh. Anke Abt holds Orthopädietechnikmeister from Meisterschule Für Orthopädietechnik.
Email format at 3R LifeScience GmbH
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AeroLeads found 1 current-domain work email signal for Anke Abt. Compare company email patterns before reaching out.
About Anke Abt
I am a process analyst and expert in making processes work 😉Let's be honest - many companies currently face: ❌ a lot of time is spent searching for necessary information and documents❌ Information is not documented or is not accessible to those who need it❌ Decisions are delayed or in many cases not made at all due to a lack of information💡 THE SOLUTION: Documented processes (SOPs) that describe clearly the scope of work, responsibilities and in- and output of information and actions to make processes work.THEREFORE: I can help you to bring structure to your existing processes and define and align interfaces, so relevant information and process data is made available to your organisation. So if you want to know✔ how to create processes that allow you to generate information ✔ how to provide information in a timely and focused manner✔ how you can make faster and better decisions as a result✔ create a smart and lean QM system in parallelWe should talk!Just send me a message directly here via Linkedin.And we'll bring your organisation to make faster and better decisions.
Anke Abt's current company
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Anke Abt work experience
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Quality Management And Regulations
CurrentDevelopment and implementation of structures and MDR-compliant processes for safe and effective medical devicesDevelopment, implementation and maintenance of QM systems according to ISO 13485 for complete quality management systemsImplementation of the EU regulation MDR 2017/745:- Review and gap analysis of existing technical documents- Preparation and adaptation of technical documentsOptimisation of R&D, QM and regulatory interfaces for a target-oriented development of medical devicesDevelopment of process landscapes and creation and review of Quality Manuals and SOPsPreparation of internal and external audits and planning of measuresCAPA processes and change management
Quality Manager
Development, optimisation and maintenance of ISO 13485 quality management processes as well as establishment of MDR-compliant technical documentationImplementation of MDR-compliant processesAudit support: MDSAP, ISO 13485Preparation of the technical documentationConducting internal auditsTraining and instruction of employeesCoordination of the digitalisation of quality-relevant processes
Quality Manager, Head Of Quality Management
Merging of 13 practice locations with different QM systems to form an overall QM system according to ISO 9001Strategic development of the QM system with the aim of scalability Consulting and reporting to the managementInterface management between the group of practices and the quality departments of the cooperating hospitalsconducting internal audits Support of certification audits as QMBControl and monitoring of error and complaint managementRequirements management for the implementation of internal knowledge data and for the administration of devices, testing/measuring equipmentTraining and instruction of shareholders and employeesMonitoring and supervision of measures from audits on compliance topics (data protection, specialist for occupational safety, hygiene, occupational medicine)Development and implementation of a uniform and scalable inspection and instruction concept in the areas of occupational safety, data protection, hygiene and occupational medical care for 13 radiology practices
Orthopädietechnikerin/-Meisterin, Qmb
Production of special medical-technical products and quality management representatives Manufacture of special medical technology productsField service, customer serviceSelection and fitting of orthopaedic aidsQuality Management Representative: Establishment of a QM system according to ISO 13585 and ISO 9001
Colleagues at 3R LifeScience GmbH
Other employees you can reach at 3r-lifescience.com. View company contacts for 7 employees →
Anke Abt education
Orthopädietechnikmeister
Orthopädietechnikerin
Frequently asked questions about Anke Abt
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What company does Anke Abt work for?
Anke Abt works for 3R LifeScience GmbH.
What is Anke Abt's role at 3R LifeScience GmbH?
Anke Abt is listed as Qualitätsmanagement, Regulations und Prozess-Digitialisierung at 3R LifeScience GmbH.
What is Anke Abt's email address?
AeroLeads has found 1 work email signal at @3r-lifescience.de for Anke Abt at 3R LifeScience GmbH.
Where is Anke Abt based?
Anke Abt is based in Berlin, Germany while working with 3R LifeScience GmbH.
What companies has Anke Abt worked for?
Anke Abt has worked for 3R Lifescience Gmbh, Dreve Prodimed Gmbh, Ranova Überörtliche Gemeinschaftspraxis Für Radiologie Und Nuklearmedizin Gbr, and Richts & Chedor Gmbh & Co. Kg.
Who are Anke Abt's colleagues at 3R LifeScience GmbH?
Anke Abt's colleagues at 3R LifeScience GmbH include Michaela Hajek, Sarah S., and Dr.-Ing. Janin Leuckert.
How can I contact Anke Abt?
You can use AeroLeads to view verified contact signals for Anke Abt at 3R LifeScience GmbH, including work email, phone, and LinkedIn data when available.
What schools did Anke Abt attend?
Anke Abt holds Orthopädietechnikmeister from Meisterschule Für Orthopädietechnik.
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